CN104046053A - Disperse fluorescent dye, preparation and application thereof - Google Patents
Disperse fluorescent dye, preparation and application thereof Download PDFInfo
- Publication number
- CN104046053A CN104046053A CN201410237950.6A CN201410237950A CN104046053A CN 104046053 A CN104046053 A CN 104046053A CN 201410237950 A CN201410237950 A CN 201410237950A CN 104046053 A CN104046053 A CN 104046053A
- Authority
- CN
- China
- Prior art keywords
- ethyl
- preparation
- fluorescent dye
- application
- dye
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
Landscapes
- Coloring (AREA)
Abstract
The invention discloses a disperse fluorescent dye, a preparation method and application thereof. The disperse fluorescent dye is a compound with a structure shown as the following general formula (I). The disperse fluorescent dye provided by the invention has the advantages of simple preparation process, good fluorescent effect, bright color, excellent application performance and convenient use, and has strong applicability.
Description
Technical field
The present invention relates to a kind of fluorescence dye, particularly relate to a kind of dispersion fluorescence dye preparation and application.
Background technology
The visual effect of fluorescence dye had both comprised the color to visible light selective absorption rear generation, comprised again the fluorescence that they emit.It belongs to a kind of Functional dye, has both had the tinctorial property of conventional dyestuff, can launch fluorescence again, and the saturation ratio of fabric and vividness are improved.Benzimidizole derivatives can be launched stronger fluorescence in organic solvent and the aqueous solution, therefore people utilize the characteristic that its fluorescence quantum yield is higher, be applied to differentiate and analyze organic compound, medicine, and for the fluorescent mark of biomacromolecule.Have in the market DISPERSE YELLOW 8GFF and the cationic yellow X-10GFF of benzimidizole derivatives structure.
Summary of the invention
Technical problem to be solved by this invention is to provide a kind of dispersion fluorescence dye of vinylbenzene benzimidazole structure, can dye to polyster fibre, yarn and fabric, is used for preparing fluorescent fiber, yarn and fabric.Particularly, the invention provides the compound of lower formula I:
(Ⅰ)
This compou nd synthesis method comprises the steps:
In propyl carbinol, adding N-Ethyl-2-Methyl benzoglyoxaline and N-ethyl-N-cyanoethyl-4-aminobenzaldehyde is raw material, acetic anhydride is catalyzer, in molar ratio, N-Ethyl-2-Methyl benzoglyoxaline, N-ethyl-N-cyanoethyl-4-aminobenzaldehyde and acetic anhydride 1:1:0.1~1.2:1:0.1, in temperature, be to react 10~12 hours under the condition of 100~105 ℃, through column chromatography for separation, obtain compound (I).
This dyestuff to dyeing terylene technique is: compound (I) consumption 0.05~10% (o.w.f, to fabric weight), bath raio 1:20~1:100, vinegar acid for adjusting pH value 4~5, room temperature enters to dye, and 2 ℃/min is warmed up to 120~135 ℃, insulation 40~60min, dyes completely, washes, soaps, washes.
Accompanying drawing explanation
Fig. 1 is for disperseing the structure iron of fluorescence dye.
Embodiment
To the present invention, disperse structure, preparation method and the application of fluorescence dye to be illustrated above, below will be by embodiment to work further instruction of the present invention.
embodiment 1:
The present embodiment provides the preparation method of formula I compound:
Concrete preparation method is as follows:
In propyl carbinol, adding N-Ethyl-2-Methyl benzoglyoxaline 8g and N-ethyl-N-cyanoethyl-4-aminobenzaldehyde 10g is raw material, 0.5g acetic anhydride is catalyzer, in temperature, be to react 12 hours under the condition of 100 ℃, through column chromatography for separation (silicagel column, sherwood oil: ethyl acetate=2:1), obtain compound (I).
embodiment 2:
The present embodiment provides the dyeing process of formula I compound to polyester piece good:
Concrete dyeing process is as follows:
Compound (I) consumption 2.0% (o.w.f, to fabric weight), bath raio 1:50, vinegar acid for adjusting pH value 5, room temperature enters to dye, and 2 ℃/min is warmed up to 130 ℃, and insulation 60min, dyes completely, washes, soaps, washes.Dye uptake 96.4%.
The prepared dispersion fluorescence dye application performance of the present invention is as follows:
Claims (3)
1. disperse a fluorescence dye, it is characterized in that its structural formula of compound is:
。
2. the preparation method of the dispersion fluorescence dye as described in claim 1, it is characterized in that comprising the steps: adding in propyl carbinol N-Ethyl-2-Methyl benzoglyoxaline and N-ethyl-N-cyanoethyl-4-aminobenzaldehyde is raw material, acetic anhydride is catalyzer, in molar ratio, N-Ethyl-2-Methyl benzoglyoxaline, N-ethyl-N-cyanoethyl-4-aminobenzaldehyde and acetic anhydride 1:1:0.1~1.2:1:0.1, in temperature, be to react 10~12 hours under the condition of 100~105 ℃, through column chromatography for separation, obtain disperseing fluorescence dye.
3. an application for the dispersion fluorescence dye as described in claim 1, is characterized in that as dispersed dye, polyster fibre, yarn or fabric being dyeed.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201410237950.6A CN104046053A (en) | 2014-06-02 | 2014-06-02 | Disperse fluorescent dye, preparation and application thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201410237950.6A CN104046053A (en) | 2014-06-02 | 2014-06-02 | Disperse fluorescent dye, preparation and application thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
CN104046053A true CN104046053A (en) | 2014-09-17 |
Family
ID=51499468
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201410237950.6A Pending CN104046053A (en) | 2014-06-02 | 2014-06-02 | Disperse fluorescent dye, preparation and application thereof |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN104046053A (en) |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5374512A (en) * | 1992-12-24 | 1994-12-20 | Konica Corporation | Silver halide photographic emulsion |
CN1821246A (en) * | 2006-03-16 | 2006-08-23 | 云南师范大学 | A class of pyrrolo-naphthyridine derivatives |
CN103525117A (en) * | 2013-10-30 | 2014-01-22 | 苏州大学 | Hemicyanine fluorescent dye and preparation method and application thereof |
-
2014
- 2014-06-02 CN CN201410237950.6A patent/CN104046053A/en active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5374512A (en) * | 1992-12-24 | 1994-12-20 | Konica Corporation | Silver halide photographic emulsion |
CN1821246A (en) * | 2006-03-16 | 2006-08-23 | 云南师范大学 | A class of pyrrolo-naphthyridine derivatives |
CN103525117A (en) * | 2013-10-30 | 2014-01-22 | 苏州大学 | Hemicyanine fluorescent dye and preparation method and application thereof |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN105623643B (en) | A kind of preparation method of composite fluorescence pigment | |
WO2013008201A3 (en) | Novel reactive dyes, there mixtures and processes thereof | |
CN104264510A (en) | Dyeing method of indigo pigment dying silk fabric | |
CN106496065B (en) | A kind of o-phenylenediamine Schiff base derivatives and the preparation method and application thereof | |
CN105133378B (en) | A kind of polyimide fiber product disperse dyeing dyeing accelerant | |
CN104448930B (en) | Reactive dye and preparation method thereof | |
CN104046053A (en) | Disperse fluorescent dye, preparation and application thereof | |
CN105418453A (en) | Process for diazotizing azo-dye intermediate | |
CN102391678A (en) | Natural dye | |
CN104046055B (en) | A kind of hair reactive fluorescent dye, preparations and applicatio | |
CN105254517A (en) | Naphthalene ring compound and preparation method thereof | |
RU2493306C1 (en) | Method of mordant dyeing of woolen fabric with vegetable dye of musk thistle | |
Otutu et al. | Synthesis of disazo disperse dye compounds derived from 4-bromoaniline and 3-aminophenol as potential near infra-red absorbers. | |
CN100503966C (en) | Perspiration-light compound fastness enhancing agent and its application | |
CN105131645A (en) | Reactive fluorescent dye for cotton, and preparation method and application thereof | |
CN103952004B (en) | A kind of high temperature modification Disperse Brown dye composition and preparation method thereof | |
CN113666939B (en) | Photochromic compound and preparation method and application thereof | |
Sunthankar et al. | Disperse dyes: dyeing properties and fastness of azo dyes | |
CN105111775A (en) | Application of azo compound | |
Liu et al. | Synthesis and dyeing performance of N, N-bis (2-cyanoethyl)-m-methylaniline disperse dyes | |
GB561117A (en) | Manufacture of metallisable or metallised direct dyestuffs | |
US1973025A (en) | Acid wool dyestuff of the anthraquinone series | |
CN105218396A (en) | A kind of preparation method of azo-compound | |
CN104710838B (en) | Disperse dye | |
CN103183657A (en) | Synthesis method of rhodamine esterification derivative |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C02 | Deemed withdrawal of patent application after publication (patent law 2001) | ||
WD01 | Invention patent application deemed withdrawn after publication |
Application publication date: 20140917 |